Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10481151
rs10481151
1 8 123819594 downstream gene variant T/C snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs10498514
rs10498514
1 14 64432337 intron variant A/C snv 7.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs11856323
rs11856323
1 15 68600650 intron variant C/T snv 8.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs1206397
rs1206397
1 2 51440601 intron variant C/A snv 3.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs17122693
rs17122693
1 14 50617517 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs17718580
rs17718580
1 14 50506914 intron variant C/T snv 7.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs1876040
rs1876040
1 2 18953470 intergenic variant A/G snv 4.3E-02 0.700 1.000 1 2010 2010
dbSNP: rs1897031
rs1897031
1 15 54049268 non coding transcript exon variant G/A snv 0.85 0.700 1.000 1 2009 2009
dbSNP: rs2179965
rs2179965
1 1 88336329 intron variant A/G snv 0.17 0.700 1.000 1 2007 2007
dbSNP: rs2203512
rs2203512
1 16 27045134 intergenic variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2229741
rs2229741
1 21 14967968 synonymous variant C/T snv 0.50 0.54 0.700 1.000 1 2009 2009
dbSNP: rs2247572
rs2247572
1 8 72720793 intron variant C/T snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs2326017
rs2326017
1 17 48643203 intron variant C/T snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs234720
rs234720
1 21 43025182 intron variant C/T snv 0.43 0.700 1.000 1 2010 2010
dbSNP: rs2484873
rs2484873
1 10 24346027 intron variant A/G snv 0.88 0.700 1.000 1 2010 2010
dbSNP: rs3744064
rs3744064
1 17 77215126 3 prime UTR variant C/T snv 2.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs4668356
rs4668356
1 2 170965956 synonymous variant C/G;T snv 2.2E-03; 0.92 0.700 1.000 1 2009 2009
dbSNP: rs5934953
rs5934953
1 X 11030572 intron variant T/C snv 2.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs6799705
rs6799705
1 3 35940638 intergenic variant C/T snv 7.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs7151223
rs7151223
1 14 48095753 intergenic variant G/A snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs7658637
rs7658637
1 4 82578160 downstream gene variant C/T snv 2.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs767210
rs767210
1 13 110817691 upstream gene variant G/A snv 9.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs7729273
rs7729273
1 5 7227934 intron variant C/T snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs8020441
rs8020441
1 14 50704161 downstream gene variant T/C;G snv 0.700 1.000 1 2010 2010